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Optics Letters|November 4, 2025
Channel-response-aware delta-sigma modulator design for low-resolution DAC-based pre-equalization systemsLinsheng Zhong, Yuming Zhao, Sunningchang Zhang, et al.
Frontiers in Genetics|November 3, 2025
A novel dinucleotide variant at 5' splice sites in the F8 gene causes exon 19 skipping in a Chinese family with hemophilia AXunzhao Zhou, Qi Yang, Qiuli Chen, et al.
Cell Discovery|September 15, 2021
Single-cell RNA-Seq reveals transcriptional heterogeneity and immune subtypes associated with disease activity in human myasthenia gravisWanlin Jin, Qi Yang, Yuyao Peng, et al.
BMC Gastroenterology|August 1, 2025
Effect of plasma adsorption and low-volume plasma exchange on intracranial pressure in acute-on-chronic liver failure: a prospective observational studyYuanji Ma, Ziyan Li, Yan Xu, et al.
Smart Molecules : Open Access|July 8, 2025
Recent advances in dual response molecular probes for biothiolsMaster Mwafulirwa, Khamis Abdalla, Wenhai Bian, et al.
European Journal of Nuclear Medicine and Molecular Imaging|July 9, 2025
ImmunoPET imaging of c-Met using a nanobody-based tracer [68Ga]Ga-NOTA-PFCM01 in pancreatic ductal adenocarcinoma models and non-human primatesXinyao Sun, Qi Yang, Lele Song, et al.
Foods (Basel, Switzerland)|December 11, 2025
Random Forest-Assisted Widely Targeted Lipidomic Reveals Differences in Tan Lamb Meat Quality in Different RegionsQi Yang, Chongxin Liu, Muxuan Xu, et al.
Molecular Genetics & Genomic Medicine|November 29, 2025
Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese FamilyQi Yang, Wei He, Qiang Zhang, et al.
Animals : an Open Access Journal From MDPI|December 17, 2024
The Effects of Lactobacillus plantarum, Bacillus subtilis, a Lignocellulolytic Enzyme System, and Their Combination on the Fermentation Profiles, Chemical Composition, Bacterial Community, and In Situ Rumen Digestion of Fresh Waxy Corn Stalk SilageJiaqi Su, Ye Xue, Kunlun Zhang, et al.
Frontiers in Genetics|December 25, 2024
Whole-exome sequencing identified a novel heterozygous variant in UBAP2L in a Chinese family with neurodevelopmental disorder characterized by impaired language, behavioral abnormalities, and dysmorphic faciesQi Yang, Qiang Zhang, Xunzhao Zhou, et al.
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